Holbrook A M, Crowther R, Lotter A, Cheng C, King D
Centre for Evaluation of Medicines, St. Joseph's Hospital, Hamilton, Ont.
CMAJ. 2000 Jan 25;162(2):225-33.
To systematically review the benefits and risks associated with the use of benzodiazepines to treat insomnia in adults.
MEDLINE and the Cochrane Controlled Trials Registry were searched for English-language articles published from 1966 to December 1998 that described randomized controlled trials of benzodiazepines for the treatment of insomnia. Key words included "benzodiazepines" (exploded), "randomized controlled trial" and "insomnia." Bibliographies of relevant articles were reviewed for additional studies and manufacturers of benzodiazepines were asked to submit additional randomized controlled trial reports not in the literature.
Articles were considered for the meta-analysis if they were randomized controlled trials involving patients with insomnia and compared a benzodiazepine with placebo or another active agent. Of the 89 trials originally identified, 45 met our criteria, representing a total of 2672 patients.
Data were extracted regarding the participants, the setting, details of the intervention, the outcomes (including adverse effects) and the methodologic quality of the studies.
The meta-analyses of sleep records indicated that, when compared with placebo, benzodiazepines decreased sleep latency by 4.2 minutes (non-significant; 95% confidence interval (CI -0.7 to 9.2) and significantly increased total sleep duration by 61.8 minutes (95% CI 37.4 to 86.2). Patient-reported outcomes were more optimistic for sleep latency; those randomized to benzodiazepine treatment estimated a sleep latency decrease of 14.3 minutes (95% CI 10.6 to 18.0). Although more patients receiving benzodiazepine treatment reported adverse effects, especially daytime drowsiness and dizziness or light-headedness (common odds ratio 1.8, 95% CI 1.4 to 2.4), dropout rates for the benzodiazepine and placebo groups were similar. Cognitive function decline including memory impairment was reported in several of the studies. Zopiclone was not found to be superior to benzodiazepines on any of the outcome measures examined.
The use of benzodiazepines in the treatment of insomnia is associated with an increase in sleep duration, but this is countered by a number of adverse effects. Additional studies evaluating the efficacy of nonpharmacological interventions would be valuable.
系统评价使用苯二氮䓬类药物治疗成人失眠的益处和风险。
检索MEDLINE和Cochrane对照试验注册库,查找1966年至1998年12月发表的描述苯二氮䓬类药物治疗失眠的随机对照试验的英文文章。关键词包括“苯二氮䓬类药物”(展开)、“随机对照试验”和“失眠”。查阅相关文章的参考文献以寻找其他研究,并要求苯二氮䓬类药物制造商提交文献中未有的其他随机对照试验报告。
如果文章是涉及失眠患者的随机对照试验,并将苯二氮䓬类药物与安慰剂或另一种活性剂进行比较,则考虑纳入荟萃分析。在最初确定的89项试验中,45项符合我们的标准,共涉及2672名患者。
提取有关参与者、研究背景、干预细节、结果(包括不良反应)以及研究方法学质量的数据。
睡眠记录的荟萃分析表明,与安慰剂相比,苯二氮䓬类药物使入睡潜伏期缩短4.2分钟(无统计学意义;95%置信区间[CI]为-0.7至9.2),并使总睡眠时间显著增加61.8分钟(95%CI为37.4至86.2)。患者报告的入睡潜伏期结果更为乐观;随机接受苯二氮䓬类药物治疗的患者估计入睡潜伏期缩短14.3分钟(95%CI为10.6至18.0)。虽然接受苯二氮䓬类药物治疗的患者报告不良反应的更多,尤其是日间嗜睡、头晕或头昏眼花(共同比值比为1.8,95%CI为1.4至2.4),但苯二氮䓬类药物组和安慰剂组的脱落率相似。多项研究报告了包括记忆损害在内的认知功能下降。在任何所检查的结果指标上,未发现佐匹克隆优于苯二氮䓬类药物。
使用苯二氮䓬类药物治疗失眠与睡眠时间增加有关,但这被一些不良反应所抵消。评估非药物干预疗效的更多研究将很有价值。